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Novaplus

FDA UDI

Class I (US FDA UDI)

by Ansell Healthcare Product

Identity

Trade Name
NOVAPLUS FDA UDI
Generic Name
Polychloroprene surgical glove, non-powdered FDA UDI
Device Name
NOVAPLUS® GAMMEX® Non-Latex Sensitive Size 6, Sterile Neoprene Powder-Free Surgical Glove FDA UDI
Model / Reference
V20277260 FDA UDI
Description
NOVAPLUS® GAMMEX® Non-Latex Sensitive Size 6, Sterile Neoprene Powder-Free Surgical Glove FDA UDI

Identifiers

Catalog Number
V20277260 FDA UDI
Primary DI / UDI-DI
10014566100606 FDA UDI
FDA Product Code
KGO FDA UDI
GMDN Term
Polychloroprene surgical glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4460 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polychloroprene surgical glove, non-powdered

Novaplus by Ansell Healthcare Product — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polychloroprene surgical glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 868efe0f-d0f8-49fe-a71b-ee783dabb064 36 fields · synced May 31, 2026